Areas of Focus
- 人类基因组拷贝数变异(CNV)及其与出生缺陷、不孕不育等疾病的关系
Publications
- TBX6 Null Variants and a Common Hypomorphic Allele in Congenital Scoliosis, Wu N, Ming X, Xiao J, Wu Z, Chen X, Shinawi M, Shen Y, Yu G, Liu J, Xie H, Gucev ZS, Liu S, Yang N, Al-Kateb H, Chen J, Zhang J, Hauser N, Zhang T, Tasic V, Liu P, Su X, Pan X, Liu C, Wang L, Shen J, Shen J, Chen Y, Zhang T, Zhang J, Choy KW, Wang J, Wang Q, Li S, Zhou W, Guo J, Wang Y, Zhang C, Zhao H, An Y, Zhao Y, Wang J, Liu Z, Zuo Y, Tian Y, Weng X, Sutton VR, Wang H, Ming Y, Kulkarni S, Zhong TP, Giampietro PF, Dunwoodie SL, Cheung SW, Zhang X, Jin L, Lupski JR, Qiu G, Zhang F, 2015
- CNV instability associated with DNA replication dynamics: evidence for replicative mechanisms in CNV mutagenesis, Chen L, Zhou W, Zhang C, Lupski JR, Jin L, Zhang F, 2015
- Replicative mechanisms of CNV formation preferentially occur as intrachromosomal events: evidence from Potocki-Lupski duplication syndrome, Sun Z, Liu P, Jia X, Withers MA, Jin L, Lupski JR, Zhang F, 2013
- Copy number variation in human health, disease, and evolution, Zhang F, Gu W, Hurles ME, Lupski JR, 2009
- The DNA replication FoSTeS/MMBIR mechanism can generate human genomic, genic, and exonic complex rearrangements, Zhang F, Khajavi M, Connolly AM, Towne CF, Batish SD, Lupski JR, 2009
Awards
- 第十五届中国青年科技奖(2019)
- 教育部高等学校自然科学一等奖(第一完成人)(2018)
- “转化医学奖励计划”转化医学创新奖(2018)
- 药明康德生命化学杰出成就奖(2015)
- 盖茨基金会“大挑战2015·青年科学家”(2015)